Holbrook T W, Spitalny G L, Palczuk N C
J Parasitol. 1976 Oct;62(5):670-5.
Mice received a series of injections of formalin-killed merozoites (FKM) of exoerythrocytic stages of Plasmodium fallax prior to challenge with sporozoites of P. berghei. In one study 4 of 16 FKM-immunized mice never exhibited parasitized erythrocytes after 2 challenges of 10(4) P. berghei sporozoites each, while all control animals died with high parasitemias. FKM-immunized mice were as susceptible as control mice to infections initiated with parasitized erythrocytes. In a second study, 14 of 16 mice immunized via the intravenous (i.v.) or combined intramuscular (i.m.) and i.v. routes were immune to an initial challenge with 10(4) sporozoites, but were susceptible to a second challenge. Three injections of FKM via the i.m. or intraperitoneal routes did not elicit a protective response against sporozoite challenge. Sera harvested from FKM-immunized and control mice prior to challenge produced no visible CSP reaction with P. berghei sporozoites, nor was infectivity of sporozoites altered after incubation in sera, showing that SNA was absent. In additional experiments results were less encouraging. An attempt to repeat the result of the second experiment failed. Each of 5 mice which received the same number of FKM by a similar schedule became infected after sporozoite challenge. In an additional study the immunization schedule was increased from 3 to 7 injections of FKM and 40% of FKM-immunized mice resisted challenge. However, mice which had received FKM prior to sporozoite challenge consistently displayed an increased prepatent period compared with control animals. A department from methods of the more successful studies was necessitated in these later studies in which FKM were harvested from cell cultures maintained for longer periods of time.
在用伯氏疟原虫子孢子攻击之前,小鼠接受了一系列福尔马林灭活的法氏疟原虫红细胞外期裂殖子(FKM)注射。在一项研究中,16只接受FKM免疫的小鼠中有4只在每次接受10⁴个伯氏疟原虫子孢子的两次攻击后,从未出现过被寄生的红细胞,而所有对照动物都因高寄生虫血症死亡。接受FKM免疫的小鼠对用被寄生的红细胞引发的感染与对照小鼠一样敏感。在第二项研究中,通过静脉内(i.v.)或肌肉内(i.m.)和静脉内联合途径免疫的16只小鼠中有14只对10⁴个子孢子的初次攻击具有免疫力,但对第二次攻击敏感。通过肌肉内或腹腔内途径注射三次FKM并未引发针对子孢子攻击的保护性反应。在攻击前从接受FKM免疫和对照小鼠采集的血清与伯氏疟原虫子孢子没有产生可见的CSP反应,并且子孢子在血清中孵育后其感染性也没有改变,表明不存在SNA。在其他实验中,结果不太令人鼓舞。重复第二项实验结果的尝试失败了。按照相似方案接受相同数量FKM的5只小鼠在子孢子攻击后均被感染。在另一项研究中,免疫方案从3次FKM注射增加到7次,40%接受FKM免疫的小鼠抵抗了攻击。然而,在子孢子攻击前接受FKM的小鼠与对照动物相比,潜伏期持续延长。在这些后期研究中,由于FKM是从维持较长时间的细胞培养物中收获的,因此需要更成功的研究方法。